Hydrogen Sulphide Compounds

ABSTRACT

The application describes Hydrogen Sulphide (H 2 S), or a (H 2 S) generating compound or compound capable of stimulating H 2 S production in a pregnant subject, for use in the treatment of pre-eclampsia (PE) or fetal growth restriction.

The invention relates to methods of treating pre-eclampsia or impaired fetal growth and to methods of monitoring such treatment, wherein the production of hydrogen sulphide (H₂S) is generated or stimulated, or is provided.

Hydrogen sulphide (H₂S), a gaseous signaling molecule, promotes vasodilatation¹ and stimulates angiogenesis in the vasculature² H₂S anti-inflammatory properties³ and is also cytoprotective against cellular damage induced by lethal hypoxia or reperfusion injury.^(4, 5) Cystathionine γ-lyase (CSE) is the principal enzyme responsible for the endogenous production of H₂S.⁶ Chronic administration of the CSE inhibitor DL-propargylglycine (PAG) leads to elevated blood pressure and vascular remodeling in the rat⁷ and both CSE and H₂S levels are reduced in pulmonary hypertensive rats.⁸ Mice genetically deficient in CSE develop age-dependent hypertension, severe hyperhomocysteinaemia, and endothelial dysfunction.⁹ Clearly H₂S has multiple roles in health and disease,^(10, 11) however its role in pregnancy-induced hypertension is unknown.

Preeclampsia is a hypertensive syndrome that affects 4-7% of all pregnancies and is a major contributor to maternal and fetal morbidity and mortality worldwide.¹² It is classified as proteinuric and non-proteinuric preeclampsia.¹³ While women with proteinuric preeclampsia exhibit the classic symptoms such as hypertension and proteinuria after 20 weeks gestation, women with non-proteinuric preeclampsia are more likely to suffer from hypertension and liver disease. Compare with gestational hypertension, these group of women are more likely to have intrauterine growth restriction (IUGR)¹³. The exact aetiology of preeclampsia is unknown, but there is a good association with abnormal placentation^(14, 15) and imbalance in angiogenic factors.^(16, 17) Importantly, circulating levels of soluble Flt-1 (sFlt-1), the endogenous inhibitor of vascular endothelial growth factor (VEGF) and placental growth factor (PlGF) as well as soluble endoglin (sEng), the cleaved product of the transforming growth factor β1 (TGF-β1) co-receptor Endoglin, are elevated several weeks prior to the onset of the clinical manifestations of preeclampsia,^(18, 19) while PlGF is reduced in the first trimester of pregnant women who subsequently developed the syndrome.²⁰⁻²⁶ Together with endothelial dysfunction, these have become the biochemical hallmark of severe preeclampsia. Few studies have investigated the functions of CSE/H₂S in pregnancy. Recently, Patel et al. demonstrated that both cystathionine β-synthase and CSE are present in human intrauterine tissues and placenta.^(27, 28) Given that the placenta is a highly vascular organ the inventors believe that the dysregulation of CSE/H₂S pathway may contribute to placental abnormalities and a preeclampsia-like condition.

The inventors have now demonstrated that plasma H₂S levels in the mother and CSE expression in the placenta are reduced in pregnancies complicated by preeclampsia as compared with gestational age matched controls. Evidence for the reduction in circulating H₂S in preeclampsia is provided and which is accompanied by down-regulation of placental CSE, the key enzyme responsible for the generation of endogenous H₂S. Inhibition of CSE activity ex vivo placental explants from first trimester (8-12 weeks) of pregnancy result in marked decrease in placenta growth factor (PlGF) production and trophoblast invasion in vitro is inhibited. Inhibition of CSE in pregnant mice induces hypertension, increases sFlt-1 and sEng levels and causes placental abnormalities due to inhibition of H₂S production as a slow releasing, H₂S-generating compound, GYY4137, restored fetal growth compromised by CSE inhibition and inhibited the rise in circulating sFlt-1 and sEng levels. These findings indicate that a dysfunctional CSE/H₂S pathway contributes to the pathogenesis of preeclampsia.

The invention provides hydrogen sulphide (H₂S), a H₂S generating compound or compound capable of stimulating H₂S production in a pregnant subject, for use in the treatment of pre-eclampsia (PE) or fetal growth restriction (FGR or intra uterine fetal growth restriction).

The invention also provides a method of treating pre-eclampsia (PE) or FGR, comprising administering to a pregnant subject a pharmaceutically effective amount of H₂S, an H₂S generating compound or a compound capable of inducing H₂S production in the subject.

The addition of H₂S has been shown to encourage, for example, angio genesis, resulting in the restoration of blood supply to the fetus.

This also means that, for example, pre-term labour may also be treated.

Pre-eclampsia, as described above, is a hypertension syndrome and a major contributor to fetal morbidity. Additionally, fetus may have impaired fetal growth due to the pregnancy induced hypertension. This “impaired fetal growth” produces lower birth weight babies and babies with increased risk of complications later.

The subject is typically a mammal, especially a human.

H₂S may be administered, for example as a gas or solution, such as in a carrier solvent.

Naturally occurring H₂S donating compounds are known. These include allicin from garlic which decomposes to diallyl disulphide and diallyl trisulphide. Sulforaphane is produce by broccoli and erucin is found in rocket (Eruca Sativa). These may be provided orally, such as in the form of tablets or capsules.

A number of synthetic H₂S compounds are known. These include GYY4137 (morpholin-4-ium 4 methoxy phenyl(morpholino)phosphinodithiolate) from Cayman Chemical. This has been previously used in rat studies to study H₂S activity by injection intraperitoneally (ip) or intravenously (iv). Lawesson's reagent is another H₂S donor.

SG1002 (Sulfa GENIX Inc) is also a H₂S producing compound and may be used. See also U.S. Pat. No. 8,361,514 B.

Anethole trithione is also a commonly used H₂S donor. Sodium sulphide in buffer (produced by Ikaria as IK-1001) has been used in clinical trails for reperfusion/injury. Other H₂S generating compounds are disclosed in Bannenberg G. L. and Viera H L A (Expert Opin. Ther. Patents (2009) 19(5) 663-682).

Other compounds are disclosed in the article by Predmore B. L. et al (Antioxidants and Redox Signalling (2012) 17 (1) 119-140), including compounds ADT-OH, TBZ and 4 hydroxyphenylisothiocyanate.

The compound may be ACS-14, AC583, ACS 84, ACS 85, ACS 86 (Lee M, J. Biol Chem (2010) 285, 17318-17328), DATS (diallyl trisulphide), S-diclofenac, sulfane sulphur, thiocysteine, GSH hydropersulphide, GYY4137, SG1002, a H₂S-donating derivative of sildenafil (ACS6-Sparatore A et al Expert Rev, Clin. Pharmacol (2011) 4, 109-121), ADT-OH, TBZ and 4-hydroxyphenyl isothiocyanate, thioglycine, 1-thiolysine, 1-thiovaline or salts thereof.

Other compounds of interest include H₂S-Latanoprost, H₂S-sildenafil, H₂S-Sartans, or H₂S-L-DOPA and derivatives of any of these.

Alternatively, the production of H₂S may be induced in the body for example by inducing CSE production or inducing other enzymes that produce H₂S in the body. For example, statins, such as simvastatin or pravastatin have been found to upregulate CSE production.

The compounds may be introduced by any suitable means, including ip, iv, orally, intrauterine for example as a pessary, or intramuscularly. They may be administered together with one or more pharmaceutically acceptable carriers or excipients. Typical doses may be 10 mmol/kg to 0.01 mol/kg, typically 10 mmol/kg to 0.1 mmol/kg.

Methods of monitoring treatment of pre-eclampsia or impaired fetal growth, comprising measuring the amount of H₂S in a sample of blood, serum or plasma in a subject prior to treatment with H₂S, or compound as described above and comparing it to the amount in a sample taken after treatment. Pre-term labour treatment may be similarly monitored.

This allows the amount of H₂S in the body to be subject to ensure that optimal levels of H₂S are provided. The amount of H₂S detected may be detected by techniques generally known in the art, such as the assay method described below.

The subject may have been treated with a compound as described above or alternatively another unrelated anti-PE as anti-impaired fetal growth compound.

The invention will now be described by way of example only with reference to the following Figures:

FIG. 1. CSE expression and H₂S levels in preeclampsia.

FIG. 2. Effects of CSE inhibition on angiogenesis factor release from human 1st trimester placenta.

FIG. 3. CSE modulates sFlt-1 and sEng release in endothelial cells.

FIG. 4. H₂S rescues preeclamptic sera-induced inhibition of in vitro tube formation.

FIG. 5. Inhibition of CSE reduces endogenous circulating H₂S and promotes hypertension and abnormal placental vascularisation in pregnant mice.

FIG. 6. H₂S-generating compound, GYY4137 restored fetal growth and inhibits sFlt-1 and sEng induced by CSE inhibition in pregnant mice.

FIG. 7. Effect of inhibition of CSE on trophoblast cell invasion.

FIG. 8. H₂S donor restores placental vascularisation in pregnant mice.

MATERIALS AND METHODS Placental Tissue Collection and Preparation

Institutional Ethics Committee approved the blood and tissue collection and written informed consent was obtained. We analysed blood samples from women with singleton pregnancies recruited in the Low- and High-Risk Clinics and Labour and Delivery Unit. All women were followed prospectively from enrolment until delivery. Human placental tissues were collected from pregnancies complicated by preeclampsia and uncomplicated pregnancies delivered by elective Caesarean. Samples of placental tissue were processed for RNA extraction and maternal plasma from the same patients (n=14 PE and n=14 control) were used for analysis. From another set of patients placenta (n=5 PE and n=5 control) was collected for the immunohistochemical study. Preeclampsia was defined as blood pressure >140/90 mm Hg on at least 2 consecutive measurements and maternal proteinuria of at least 300 mg/24 h. First trimester placental tissues (6-9 weeks gestational age) were retrieved from normal pregnancies that had undergone elective termination. Villus explants were prepared as described previously.²⁹ Briefly, human placental villus explants were incubated with or without PAG for 24 hours, and conditioned media collected and assayed for sFlt-1 or sEng and PlGF.

Animal Experimental Protocol

Eight to ten week old C57/black6 mice were mated. The first day of pregnancy (E0.5) was defined by the presence of a vaginal plug the following morning. Pregnant mice were randomly assigned into four groups: (i) saline (vehicle control), (ii) 25 mg/kg DL-propargylglycine (PAG; Sigma, Poole, U.K.), (iii) 50 mg/kg group PAG and (iv) 50 mg/kg

PAG with 0.25 mg/kg of slow-releasing H₂S donor, GYY4137(Sigma). Mice were injected intraperitoneally (i.p.) with saline or PAG from E8.5. Blood pressure was measured by tail cuff-plethysmography. Mice were trained for measurement on alternate days from E4.5. Alternatively, mice were anesthetized by Ketamine/Xylazine cocktail. The carotid artery was isolated and cannulated with a 3-Fr high-fidelity microtip catheter connected to a pressure transducer (Millar Instruments, Houston, Tex., USA). Blood pressure was recorded and averaged over a 10-minute period. On E17.5, after blood pressure measurement and blood sample collection the animals were sacrificed and kidney, liver, and placenta were collected. The un-absorbed fetuses and placentas were counted and weighed.

All experimentation was conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act, 1986 using procedures approved by the University of Edinburgh Ethical Review Committee.

Histopathology

Kidney, liver, and placenta were immersion fixed in 4% paraformaldehyde for 24 hours and processed to paraffin. A series of 5-μm sections were cut and processed for hematoxylin & eosin (H&E) staining.

Cell Culture

Human umbilical vein endothelial cells (HUVEC) were isolated and cultured as previously described.³⁰ Experiments were performed on third or fourth passage HUVEC.

RNA Interference

To silence human CSE expression, we performed transfection of small-interfering RNA (siRNA) duplex using electroporation (Nucleofector, Amaxa). Control and CSE siRNAs were synthesized by Eurogentec (Cologne, Germany). Knockdown of CSE in HUVEC was confirmed using Western blotting.

Adenoviral Gene Transfer

The recombinant, replication-deficient adenovirus encoding human CSE (AdCSE) and empty vector (AdEV) were purified on CsCl gradients, titered, and stored at −80° C. in viral storage buffer prior to use as described previously.³¹ Optimal multiplicity of infection for AdCSE was determined to be 20 IFU/cell by Western blotting using a rabbit anti-CSE antibody (Abcam). AdEV infected HUVEC were used as a negative control.

Enzyme-Linked Immunosorbent Assay

Enzyme-linked immunosorbent assay (ELISA) kits for human and murine soluble Flt-1, soluble endoglin and PlGF were obtained from R&D Systems and performed according to the manufacturer's specifications.

Immunohistochemistry

Serial 3-5-μm sections of formalin-fixed, paraffin-embedded human and murine placental tissue were prepared for immunohistochemistry as previously described.²⁹ Biotin-labelled isolectin B4, anti-CSE (5 mg/ml) and isotype control were used. The staining was analyzed using a Nikon inverted microscope and an Image Pro Plus image analysis software (Media Cybernetics).

Real-Time Polymerase Chain Reaction (PCR)

Sample preparation and real-time quantitative PCR was performed as described previously.³⁰ Briefly, mRNA from placental tissue was extracted using TRIzol and DNase-1 digestion/purification on RNAeasy columns (Qiagen), and reverse transcribed with the cDNA Synthesis Kit (Promega). Triplicate cDNA samples and standards were amplified in SensiMix containing SYBR green (Quantace) with primers specific for CSE (GCC-CAG-TTC-CGT-GAA-TCT-AA; CAT-GCT-GAA-GAG-TGC-CCT-TA) or β-actin. The mean threshold cycle (CT) for CSE was normalized to β-actin and expressed relative to control.

In Vitro Angiogenesis Assay

The spontaneous formation of capillary-like structures by HUVECs on growth factor-reduced Matrigel (Becton Dickinson, Bedford, Mass.), was used to assess angiogenic potential. HUVECs were treated with plasma samples collected from pregnancies complicated by preeclampsia and uncomplicated pregnancies with or without H₂S donor (NaHS) and incubated at 37° C. for 24 hours. Ninety-six well plates were coated with Matrigel (10 mg/ml) according to the manufacturer's instructions. HUVECs (1×10⁴ cells/well) were then seeded on Matrigel-coated plates. After incubation for 6 hours, cells were observed with a Nikon inverted microscope and experimental results recorded using the Image Pro-Plus image analysis software (Media Cybernetics).

Measurement of H₂S in Plasma

Citrated blood was obtained from women with uncomplicated pregnancies (n=14) and preeclampsia (n=14) and also from pregnant mice before termination of pregnancy. H₂S levels were measured as described previously with modification.³² Briefly, 75 μl plasma was mixed with 250 μl of 1% (w/v) zinc acetate and 425 μl water, followed by 250 ml 50% trichloroacetic acid to remove protein. Then 133 μl 20 mM N-dimethyl-p-phenylenediamine sulphate in 7.2 mM HCl and 133 μl 30 μM FeCl₃ in 1.2 mM HCl were added to the mixture. After 10 min incubation at room temperature, reaction mixtures were pelleted by centrifugation at 10,000 g (2 minutes). The absorbance of the resulting solution was measured at 670 nm with a spectrophotometer in a 96-well plate. The concentration of H₂S in the solution was calculated against a calibration curve of sodium hydrogen sulfide.

Statistical Analysis

Data are expressed as mean±SEM. The significance of the difference between means was tested by non-parametric Man Whitney t-test. For statistical analysis of changes in clinical samples, one-way ANOVA was used, followed by the Student-Newman-Keuls test as appropriate. An observer blinded to treatment performed the analyses. Statistical significance was set at p<0.05.

Results Placenta CSE Expression is Reduced in Preeclampsia

To investigate whether CSE/H₂S activity is altered in preeclampsia, H₂S was measured in plasma obtained from gestational age-matched control pregnancies and those complicated by preeclampsia. Maternal plasma H₂S levels were significantly reduced in preeclampsia compared with controls group (FIG. 1A). Quantitative real-time PCR revealed that the CSE mRNA expression was significantly reduced in preeclamptic placenta (FIG. 1B) and immunohistochemical staining confirmed that CSE immunoreactiovity was dramatically reduced in these samples (FIG. 1C iv) suggesting that the changes in placental CSE levels affect maternal circulating H₂S levels. Expressed of CSE was located in the trophoblast, the endothelium and the mesenchymal cells within the core of the chorionic villus. The latter are possibly the Hofbauer cells, which are of mesenchymal origin (FIG. 1C iii). Clinical characteristics of the study patients are described in Table 1.

Inhibition of CSE Activity Reduces PlGF Release in Placental Explants

Angiogenic factors produced by placenta are important in regulating placental vascular development.³³ Imbalance of pro- and anti-angiogenic factors generated by the placenta²⁹ may account for the widespread maternal endothelial dysfunction in preeclampsia.³⁴ To investigate whether reduced levels of CSE has any effect on the production of placental angiogenic factor production, sFlt-1, sEng, and PlGF levels were measured in conditioned medium from first trimester human placental explants in the presence of increasing concentration of CSE inhibitor PAG over 24 hours. While the levels of sFlt-1 and sEng remained unchanged by the inhibition of CSE activity, PlGF production was significantly reduced (FIG. 2). This suggests that reduction in endogenous H₂S may alter the placental sFlt-1/PlGF ratio, which has been implicated in the pathogenesis of preeclampsia.^(18, 29) In addition, a significant reduction (p<0.01) in cell invasion was observed when first trimester trophoblast cells (HTR-8/SVneo) were incubated with the CSE specific inhibitor PAG (50 μM) compared with the vehicle control (Supplemental Fig. S1A and S1B), suggesting that lack of CSE activity may affect placental perfusion which is essential for establishing normal pregnancy.

CSE Modulates sFlt-1 and sEng Release in Endothelial Cells

Although placenta has been considered to be the main source of sFlt-1 and sEng release in preeclampsia patients, some studies have shown that levels of sFlt-1 remained higher in women with a history of preeclampsia compared with those without preeclampsia an average of 18 months postpartum^(35, 36) suggesting that other antiangiogenic milieu are involved in the process. To investigate whether CSE affects sFlt-1 and sEng release in endothelial cells, CSE expression was modulated by siRNA or adenovirus in HUVECs. Down-regulation of CSE increased both sFlt-1 and sEng release (FIG. 3A, 3B) while over-expression of CSE inhibited sFlt-1 and sEng release by HUVECs (FIG. 3C, 3D). These data further support the concept that loss of CSE activity may contribute to the pathogenesis of preeclampsia.

H₂S Partially Rescues Preeclamptic Plasma-Induced Inhibition of In Vitro Tube Formation

It has been demonstrated that excess sFlt-1 generated by preeclamptic placenta inhibits in vitro endothelial tube formation and removal of sFlt-1 from preeclampsia samples restores angiogenesis.²⁹ To assess whether H₂S can reverse the anti-angiogenic effects of preeclampsia, plasma from normotensive or preeclamptic women was added to HUVEC grown on growth factor-reduced Matrigel in the presence of 100 mM NaHS, a H₂S donor, and in vitro tube formation assay performed. Consistence with earlier findings, preeclamptic plasma inhibited capillary tube network formation compare with normal control sera (FIG. 4). More importantly, NaHS, a H₂S donor, partially restored the ability of HUVECs to form tube-like structure (FIG. 4A, 4B).

Blocking Endogenous H₂S Causes Hypertension and Abnormal Placental Vascularisation in Pregnant Mice

We predicted that inhibition of CSE in vivo would cause a preeclampsia-like syndrome in pregnant mice. Three groups (5-8/group) of pregnant C57Bl6/J mice were treated daily with vehicle or 25 mg/kg PAG or 50 mg/kg PAG from E8.5 to E16.5. After 8 days of treatment, plasma was pooled from all animals in each treatment group, and pooled H₂S levels were measured. PAG caused a dose-dependent decrease in circulating H₂S levels. The higher dose reduced plasma H₂S levels by approximately 50% (FIG. 5A). In consistence of these data, we found that the mean blood pressure in high dose PAG treated group was significant higher compared with vehicle control (74.40±4.61 and 64.74±2.04) (Table 2). Although renal pathological changes such as proteinuria was not noted in our PAG treated animals (Table 2), liver damage represented by increased level of circulating liver enzyme aspartate transaminas (AST) was found in PAG-treated animals (Table 2). These date suggest that lack of CSE activity may cause non-proteinuric preeclampsia. Interestingly, all the changes of PAG-treated pregnant mice were abrogated by a slow releasing, H₂S-generating compound GYY4137 (0.25 mg/kg) treatment (Table 2). Blinded histological analysis of placental sections showed that the maternal blood space in the labyrinth zone appeared larger in 50 mg/kg PAG-treated animals than in vehicle controls (FIG. 5B). The labyrinth zone consists of cells of trophoblast and mesodermal origin that together undergo branching morphogenesis, resulting in a large surface area for nutrient and gas exchange between the mother and fetus. The maternal blood space is lined by trophoblast. During placental development, this space becomes progressively more finely divided.^(37, 38) Using isolectin B₄ to highlight the fetal endothelial cell,³⁹ we compared the anatomical features of the labyrinth zone in vehicle and 50 mg/kg PAG-treated mice. In control mice, the labyrinth appeared as organised fetal vessels with well-developed branching morphogenesis. In contrast, the fetal vasculature of the placenta in PAG-treated animals was observed as irregular branching (FIG. 5C) and maternal vasculature appear to be dilated. The morphology of placenta from PAG-treated animals suggests a placental vascular defect due to inhibition of CSE activity. This defect was also restored by H₂S donor GYY4137 treatment (Fig. S2).

The Effects of Inhibition of CSE Activity on Fetal Outcomes and sFlt-1 and sEng Production

Fetal weight was significantly decreased in mice that received the higher dose of PAG (FIG. 6A). This could be explained by placental vascular defect induced by inhibition of CSE activity. GYY4137, at 0.25 mg/kg restored fetal growth compromised by the CSE inhibitor (FIG. 6A). Furthermore, GYY4137 inhibited the plasma levels of sFlt-1 and sEng induced by CSE inhibition (FIGS. 6B and 6C) in mice treated with 50 mg/kg PAG (FIGS. 5B and 5C). Plasma PlGF was below the detection limit of the assay. These data suggest that inhibition of CSE activity alters maternal angiogenic balance and H₂S can help to restore normal angiogenic status.

Discussion

Chronic administration of a CSE inhibitor leads to reduced H₂S and increased blood pressure in rats.⁷ Thus it is plausible that a reduction in the circulating H₂S level may contribute to hypertension in preeclampsia. In this study we provide evidence that preeclampsia is associated with reduced circulating H₂S, which is accompanied by down-regulation of placental CSE, the key enzyme responsible for the generation of endogenous H₂S. Furthermore, the inhibition of CSE in pregnant mice induces hypertension, increases sFlt-1 and sEng levels and causes placental abnormalities. This is due to inhibition of H₂S production as a slow releasing, H₂S-generating compound, GYY4137, inhibited circulating sFlt-1 and sEng levels and restored fetal growth compromised by CSE inhibition. These findings indicate that a dysfunctional CSE/H₂S pathway may contribute to the pathogenesis of preeclampsia.

H₂S is a vasorelaxant factor that acts through K_(ATP) channels causing smooth muscle relaxation^(1, 40) Studies using mice genetically deficient in CSE demonstrated that this enzyme is the major source of H₂S in both the vasculature and the peripheral tissues.⁹ Recently, CSE expression was found in the placenta and pregnant myometrium and it was shown to play a role in uterine contractility.^(27, 28) In this study, placental CSE levels were dramatically reduced in preeclamptic patients compared with normotensive controls. A recent study also showed similar pattern in CSE in preeclamptic placenta.⁴¹ These findings suggest that lack of the CSE leads to the reduction in circulating H₂S.

Angiogenic imbalance has been highlighted as the prime culprit in preeclampsia over systemic inflammation.^(42, 43) In this study, CSE was found to be a negative regulator of anti-angiogenic factors, sFlt-1 and sEng, in endothelial cells, suggesting that dysregulation of CSE may contribute to the lasting endothelial dysfunction and an elevated risk of cardiovascular disease in women with a history of preeclampsia. In addition, the decrease in VEGF and PlGF activity in preeclampsia is believed to be the result of excess sFlt-1.^(16, 18) As sFlt-1 levels are comparable to healthy controls during the first trimester of pregnancy, this theory does not explain why the circulating levels of PlGF are low in early pregnancy in women who subsequently develop preeclampsia.⁴⁴ Our findings that inhibition of endogenous placental H₂S generation by CSE inhibitor attenuates the production of PlGF in first trimester placental explants provides a possible explanation and a new hypothesis for testing: namely, the decrease in PlGF expression in early pregnancy is due to loss or reduction in the enzymes producing H₂S. Furthermore, inhibition of CSE activity abolished the invasion of first-trimester extravillus trophoblast cells suggesting that dysregulation of CSE/H₂S pathway may not only change the balance of placental pro- and anti-angiogenesis factors, but also dysregulate maternal spiral artery remodeling and placental development.

In pregnant mice, CSE inhibition reduced endogenous H₂S and this was accompanied by an increase in blood pressure, and liver damage without renal pathological changes such as proteinuria and glomerular endotheliosis, a syndrome similar to non-proteinuric preeclampsia. However, it also suggests that other factors are also involved in the full spectrum of preeclampsia. Preeclampsia is also strongly associated with placental abnormalities including compromised villus volume and surface area, as well as reduced placental vascularisation.^(15, 45) In the PAG-treated mice, the fetal labyrinth showed impaired branching morphogenesis, indicating endogenous H₂S is required for placental development.

Impaired placental perfusion and suboptimal oxygen and nutrient diffusion has been reported to occur as a result of inappropriate labyrinth vascularisation with altered patterning, branching and dilation.⁴⁶ Blood pressure, liver function and fetal weight compromised by PAG-treatment were rescued by the slow releasing, H₂S-generating compound, GYY4137, demonstrating that the effects of CSE inhibitor were due to inhibition of H₂S production. These results imply that endogenous H₂S is required for healthy placental vasculature to support fetal wellbeing.

Clinical Perspective

The present study shows that dysregulation of CSE/H₂S pathway is associated with preeclampsia and inhibition of CSE activity in pregnant mice produces some of the features of preeclampsia, including hypertension and impaired fetal outcomes. These findings support the concept that H₂S is an important regulator of the placental vasculature development, a deficiency of which appears to be associated with preeclampsia and fetal growth restriction.

Supplemental Methods Trophablast Cell Invasion Assay

The human extravillus trophoblast (EVT) cell line HTR-8/SVneo was a kind gift from Professor Charles H. Graham, Queen's University, Kingston, Ontario, Canada. The invasion assay was performed as described previously, with modification.30 Briefly, HTR-8/SVneo (50,000) cells treated with or without PAG were placed in the upper chamber of Matrigel-coated (1 mg/ml) transwell inserts (8 μm pore, Falcon, BD, UK) and housed in a 24-well plate. The cells were allowed to invade through the reconstituted extracellular matrix for 24 h in the presence or absence of 50 M PAG (n=3). Trophoblast cells located on the under-surface of the transwell membrane were fixed with ice-cold methanol and stained with hematoxylin, and brightfield images were obtained with Nikon inverted microscope and Image Pro Plus image analysis software (Media Cybernetics).

Immunohistochemistry

Serial 3-5-μm sections of formalin-fixed, paraffin-embedded murine placental tissue were prepared for immunohistochemistry as previously described⁴⁸. Biotin-labelled isolectin B4, were used. The staining was analyzed using a Nikon inverted microscope and an Image Pro Plus image analysis software (Media Cybernetics).

FIG. 7. Effect of Inhibition of CSE on Trophoblast Cell Invasion.

Transwell migration assays of HTR-8/SVneo cells in the presence of 50 M of PAG were performed as described in Methods. (A) Migrated HTR-8/SVneo were stained with hematoxylin, and brightfield images were captured. (B) Cell numbers were counted, and results are expressed as a percentage of the control (n=3).

FIG. 8. H₂S Donor Restores Placental Vascularisation in Pregnant Mice.

Placental tissue from mice received either (A) PAG 50 mg/kg or (B) PAG 50 mg/kg plus GYY4137 injection were sectioned and stained with Isolectin B₄ to visualize haemotrichorial labyrinth zone.

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1.-6. (canceled)
 7. A method for treating pre-eclampsia or fetal growth restriction in a host animal, the method comprising administering to the host animal an effective amount of one or more compounds selected from the group consisting of H₂S, a compound capable of generating H₂S, a compound capable of stimulating H₂S in the host animal, or a combination thereof.
 8. The method of claim 1 wherein the compound is H₂S, ACS 14, AC583, ACS 84, ACS 85, ACS 86, DATS, S-diclofenac, sulfane sulfur, thiocysteine, GSH hydropersulfide, GYY4137, SGI 002, a H₂S-donating derivative of sildenafil, ADT-OH, TBZ and 4-hydroxyphenyl isothiocyanate, thioglycine, 1-thiolysine, 1-thiovaline or a salt thereof, H₂S-Latanoprost or a derivative thereof, H₂S-sildenafil or a derivative thereof, H₂S-Sartans or a derivative thereof, H₂S-L-DOPA or a derivative thereof, or a combination thereof.
 9. A method for treating pre-term labor in a pregnant host animal, the method comprising administering to the host animal an effective amount of one or more compounds selected from the group consisting of H₂S, a compound capable of generating H₂S, a compound capable of inducing H₂S production in the host animal, or a combination thereof.
 10. The method of claim 9 wherein the compound is H₂S, ACS 14, AC583, ACS 84, ACS 85, ACS 86, DATS, S-diclofenac, sulfane sulfur, thiocysteine, GSH hydropersulfide, GYY4137, SGI 002, a H₂S-donating derivative of sildenafil, ADT-OH, TBZ and 4-hydroxyphenyl isothiocyanate, thioglycine, 1-thiolysine, 1-thiovaline or a salt thereof, H₂S-Latanoprost or a derivative thereof, H₂S-sildenafil or a derivative thereof, H₂S-Sartans or a derivative thereof, H₂S-L-DOPA or a derivative thereof, or a combination thereof.
 11. A method for monitoring treatment of pre-eclampsia or impaired fetal growth in a host animal, the method comprising measuring the amount of H₂S in the blood, serum or plasma of the host animal prior to treatment and comparing it to the amount of H₂S after treatment.
 12. The method of claim 11 further comprising treating the host animal with one or more compounds selected from the group consisting of H₂S, a compound capable of generating H₂S, a compound capable of stimulating H₂S production in the host animal, or a combination thereof.
 13. The method of claim 12 wherein the compound is H₂S, ACS 14, AC583, ACS 84, ACS 85, ACS 86, DATS, S-diclofenac, sulfane sulfur, thiocysteine, GSH hydropersulfide, GYY4137, SGI 002, a H₂S-donating derivative of sildenafil, ADT-OH, TBZ and 4-hydroxyphenyl isothiocyanate, thioglycine, 1-thiolysine, 1-thiovaline or a salt thereof, H₂S-Latanoprost or a derivative thereof, H₂S-sildenafil or a derivative thereof, H₂S-Sartans or a derivative thereof, H₂S-L-DOPA or a derivative thereof, or a combination thereof. 